Please use this identifier to cite or link to this item: https://doi.org/10.1039/c1ob05881a
Title: Enantioselective Morita-Baylis-Hillman reaction promoted by l-threonine-derived phosphine-thiourea catalysts
Authors: Han, X.
Wang, Y.
Zhong, F.
Lu, Y. 
Issue Date: 7-Oct-2011
Citation: Han, X., Wang, Y., Zhong, F., Lu, Y. (2011-10-07). Enantioselective Morita-Baylis-Hillman reaction promoted by l-threonine-derived phosphine-thiourea catalysts. Organic and Biomolecular Chemistry 9 (19) : 6734-6740. ScholarBank@NUS Repository. https://doi.org/10.1039/c1ob05881a
Abstract: A series of bifunctional phosphine-thiourea organic catalysts based on natural amino acid scaffolds were designed and prepared. l-Threonine-derived bifunctional phosphine catalysts were found to be very efficient in promoting asymmetric Morita-Baylis-Hillman (MBH) reaction of acrylates with aromatic aldehydes, affording the desired MBH adducts with up to 90% ee. To gain mechanistic insights into the reaction, the effects of adding various additives on the MBH reaction were investigated. We propose that the hydrogen bonding interactions between the thiourea moiety of the catalyst and the enolate intermediate are crucial for the stereochemical outcome of the reaction. The method described in this report may provide a practical solution to the enantioselective MBH reaction of simple acrylates. © 2011 The Royal Society of Chemistry.
Source Title: Organic and Biomolecular Chemistry
URI: http://scholarbank.nus.edu.sg/handle/10635/76104
ISSN: 14770520
DOI: 10.1039/c1ob05881a
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